Have questions? Visit https://www.reddit.com/r/SNPedia

rs9261129

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9261129(C;C)
Make rs9261129(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30011802
GeneHCG8
is asnp
is mentioned by
dbSNPrs9261129
ebirs9261129
HLIrs9261129
Exacrs9261129
Varsomers9261129
Maprs9261129
PheGenIrs9261129
hapmaprs9261129
1000 genomesrs9261129
hgdprs9261129
ensemblrs9261129
gopubmedrs9261129
geneviewrs9261129
scholarrs9261129
googlers9261129
pharmgkbrs9261129
gwascentralrs9261129
openSNPrs9261129
23andMers9261129
23andMe allrs9261129
SNP Nexus

SNPshotrs9261129
SNPdbers9261129
MSV3drs9261129
GWAS Ctlgrs9261129
GMAF0.1846
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 18495769OA-icon.png] Transmission of human immunodeficiency virus type 1 from a patient who developed AIDS to an elite suppressor.


[PMID 18982067OA-icon.png] HIV-1 disease-influencing effects associated with ZNRD1, HCP5 and HLA-C alleles are attributable mainly to either HLA-A10 or HLA-B*57 alleles.


[PMID 20041166OA-icon.png] Common genetic variation and the control of HIV-1 in humans.


GET Evidence
rs9261129
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.195312
summary